Composition for organic layer of organic solar cell and organic solar cell

ABSTRACT

The present specification relates to a composition for an organic material layer of an organic solar cell including an electron donor including a polymer including a first unit represented by Chemical Formula 1, a second unit represented by Chemical Formula 2, and a third unit represented by Chemical Formula 3 or 4; and a non-fullerene-based electron acceptor, and an organic solar cell including the composition.

TECHNICAL FIELD

This application claims priority to and the benefits of Korean PatentApplication No. 10-2018-0028135, filed with the Korean IntellectualProperty Office on Mar. 9, 2018, the entire contents of which areincorporated herein by reference.

The present specification relates to a composition for an organicmaterial layer of an organic solar cell, and an organic solar cell.

BACKGROUND ART

An organic solar cell is a device capable of directly converting solarenergy to electric energy by applying a photovoltaic effect. Solar cellsare divided into inorganic solar cells and organic solar cells dependingon the materials forming a thin film. Typical solar cells are fabricatedusing a p-n junction by doping crystalline silicon (Si), an inorganicsemiconductor. Electrons and holes generated by light absorption spreadto p-n junction points, are accelerated by the electric field, andmigrate to an electrode. Power conversion efficiency of this process isdefined as a ratio of power given to an external circuit and solar powerput into a solar cell, and the ratio has been accomplished up toapproximately 24% when measured under a currently standardizedhypothetical solar irradiation condition. However, existing inorganicsolar cells already have limits in economic feasibility and materialsupplies, and therefore, organic material semiconductor solar cells thatare readily processed, inexpensive and have various functions have beenhighly favored as a long-term alternative energy source.

For solar cells, it is important to increase efficiency so as to outputas much electric energy as possible from solar energy. In order toincrease efficiency of such solar cells, generating as much excitons aspossible inside a semiconductor is important, however, taking thegenerated charges outside without loss is also important. One of thereasons for the charge loss is the dissipation of the generatedelectrons and holes by recombination. Various methods for delivering thegenerated electrons or holes to an electrode without loss have beenproposed, however, most of the methods require additional processes, andaccordingly, the fabricating costs may increase.

DISCLOSURE Technical Problem

The present specification is directed to providing a composition for anorganic material layer of an organic solar cell, and an organic solarcell including the composition.

Technical Solution

One embodiment of the present specification provides a composition foran organic material layer of an organic solar cell including an electrondonor including a polymer including a first unit represented by thefollowing Chemical Formula 1, a second unit represented by the followingChemical Formula 2, and a third unit represented by the followingChemical Formula 3 or 4; and a non-fullerene-based electron acceptor.

In Chemical Formulae 1 to 4,

X1 to X6 are the same as or different from each other, and eachindependently CRR′, NR, O, SiRR′, PR, S, GeRR′, Se or Te,

Y1 and Y2 are the same as or different from each other, and eachindependently CR″, N, SiR″, P or GeR″,

A1 and A2 are the same as or different from each other, and eachindependently a halogen group,

Cy1 is a substituted or unsubstituted heteroring,

Q1 and Q2 are the same as or different from each other, and eachindependently O or S, and

R, R′, R″ and R1 to R8 are the same as or different from each other, andeach independently hydrogen; deuterium; a halogen group; a nitrilegroup; a nitro group; an imide group; an amide group; a hydroxyl group;a substituted or unsubstituted alkyl group; a substituted orunsubstituted cycloalkyl group; a substituted or unsubstituted alkoxygroup; a substituted or unsubstituted aryloxy group; a substituted orunsubstituted alkylthio group; a substituted or unsubstituted arylthiogroup; a substituted or unsubstituted alkylsulfoxy group; a substitutedor unsubstituted arylsulfoxy group; a substituted or unsubstitutedalkenyl group; a substituted or unsubstituted amine group; a substitutedor unsubstituted aryl group; or a substituted or unsubstitutedheterocyclic group.

Another embodiment of the present specification provides an organicsolar cell including a first electrode; a second electrode disposedopposite to the first electrode; and one or more organic material layersdisposed between the first electrode and the second electrode andincluding a photoactive layer, and one or more layers of the organicmaterial layers include the composition for an organic material layer ofan organic solar cell described above.

Advantageous Effects

A polymer according to one embodiment of the present specification is anelectroconductive material, and has thermal stability, excellentsolubility and high electron mobility. Accordingly, excellent electricalproperties can be obtained when used in an organic solar cell.

In addition, the polymer according to one embodiment of the presentspecification has a high HOMO energy level, and when obtaining anorganic solar cell including the same, excellent efficiency is obtained.

By using the polymer described in embodiments of the presentspecification in an organic solar cell together with anon-fullerene-based electron acceptor, battery efficiency can beenhanced. The non-fullerene-based electron acceptor has advantages inthat an absorption wavelength region of light is readily controlledcompared to existing fullerene-based electron acceptors such as PCBM,and the absorption wavelength region can be controlled so as not tooverlap with an absorption wavelength region of an electron donorincreasing a short circuit current, and thermal stability is superiorsince an aggregation phenomenon in which electron acceptor materialsaggregate with each other occurs less compared to fullerene-basedelectron acceptors. In order to obtain favorable efficiency with such anon-fullerene-based electron acceptor, an electron donor of whichabsorption wavelength does not overlap and having proper HOMO and LUMOenergy levels needs to be used, and the polymer according to oneembodiment of the present specification satisfies such properties andcan form proper morphology with the non-fullerene-based electronacceptor.

DESCRIPTION OF DRAWINGS

FIG. 1 is a diagram illustrating an organic solar cell according to oneembodiment of the present specification.

FIG. 2 is a diagram presenting a UV-Vis spectrum of Polymer 5 in a filmstate.

FIG. 3 is a diagram presenting a UV-Vis spectrum of Polymer 13 in a filmstate.

REFERENCE NUMERAL

101: First Electrode

102: Electron Transfer Layer

103: Photoactive Layer

104: Hole Transfer Layer

105: Second Electrode

MODE FOR DISCLOSURE

Hereinafter, the present specification will be described in more detail.

In the present specification, a ‘unit’ is a repeated structure includedin a monomer of a polymer, and means a structure in which the monomerbonds in the polymer by polymerization.

In the present specification, the meaning of ‘including a unit’ meansbeing included in a main chain in a polymer.

In the present specification, a description of a certain part“including” certain constituents means capable of further includingother constituents, and does not exclude other constituents unlessparticularly stated on the contrary.

In the present specification, an energy level means energy magnitude.Therefore, even when an energy level is expressed in a negative (-)direction from a vacuum level, the energy level is interpreted to meanan absolute value of the corresponding energy value. For example, a HOMOenergy level means a distance from a vacuum level to the highestoccupied molecular orbital. In addition, a LUMO energy level means adistance from a vacuum level to the lowest unoccupied molecular orbital.

One embodiment of the present specification provides a composition foran organic material layer of an organic solar cell including an electrondonor including a polymer including a first unit represented by thefollowing Chemical Formula 1, a second unit represented by the followingChemical Formula 2, and a third unit represented by the followingChemical Formula 3 or 4; and a non-fullerene-based electron acceptor.

Particularly, the polymer includes a second unit represented by ChemicalFormula 2. In one embodiment of the present specification, A1 and A2substitute an ortho position of the benzene ring. This results in lowcrystallinity forming a small domain. Accordingly, an organic solar cellincluding the same exhibits excellent electrical properties, and hasexcellent efficiency and current properties.

Examples of the substituents are described below, however, thesubstituents are not limited thereto.

The term “substitution” means a hydrogen atom bonding to a carbon atomof a compound is changed to another substituent, and the position ofsubstitution is not limited as long as it is a position at which thehydrogen atom is substituted, that is, a position at which a substituentcan substitute, and when two or more substituents substitute, the two ormore substituents may be the same as or different from each other.

In the present specification, the term “substituted or unsubstituted”means being substituted with one or more substituents selected from thegroup consisting of deuterium; a halogen group; a nitrile group; a nitrogroup; an imide group; an amide group; a hydroxyl group; a substitutedor unsubstituted alkyl group; a substituted or unsubstituted cycloallcylgroup; a substituted or unsubstituted alkoxy group; a substituted orunsubstituted aryloxy group; a substituted or unsubstituted allcylthiogroup; a substituted or unsubstituted arylthio group; a substituted orunsubstituted alkylsulfoxy group; a substituted or unsubstitutedarylsulfoxy group; a substituted or unsubstituted alkenyl group; asubstituted or unsubstituted silyl group; a substituted or unsubstitutedboron group; a substituted or unsubstituted amine group; a substitutedor unsubstituted aryl group; and a substituted or unsubstitutedheterocyclic group, being substituted with a substituent linking two ormore substituents among the substituents illustrated above, or having nosubstituents. For example, “a substituent linking two or moresubstituents” may include a biphenyl group. In other words, a biphenylgroup may be an aryl group, or interpreted as a substituent linking twophenyl groups.

In the present specification, the number of carbon atoms of the imidegroup is not particularly limited, but is preferably from 1 to 30.Specifically, compounds having structures as below may be included,however, the imide group is not limited thereto.

In the present specification, in the amide group, the nitrogen of theamide group may be substituted once or twice with a linear, branched orcyclic alkyl group having 1 to 30 carbon atoms or an aryl group having 6to 30 carbon atoms. Specifically, compounds having the followingstructural formulae may be included, however, the amide group is notlimited thereto.

In the present specification, examples of the halogen group may includefluorine, chlorine, bromine or iodine.

In the present specification, the alkyl group may be linear or branched,and although not particularly limited thereto, the number of carbonatoms is preferably from 1 to 50. Specific examples thereof may includemethyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl,tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl,isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl,2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl,heptyl, n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl,octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl,2-propylpentyl, n-nonyl, 2,2-dimethylheptyl, 1-ethyl-propyl,1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl,5-methyihexyl and the like, but are not limited thereto.

In the present specification, the cycloalkyl group is not particularlylimited, but preferably has 3 to 60 carbon atoms. Specific examplesthereof may include cyclopropyl, cyclobutyl, cyclopentyl,3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl,3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl,3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl,cyclooctyl and the like, but are not limited thereto.

In the present specification, the alkoxy group may be linear, branchedor cyclic. The number of carbon atoms of the alkoxy group is notparticularly limited, but is preferably from 1 to 20. Specific examplesthereof may include methoxy, ethoxy, n-propoxy, isopropoxy, i-propyloxy,n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy,isopentyloxy, n-hexyloxy, 3,3-dimethylbutyloxy, 2-ethylbutyloxy,n-octyloxy, n-nonyloxy, n-decyloxy and the like, but are not limitedthereto.

In the present specification, the alkenyl group may be linear orbranched, and although not particularly limited thereto, the number ofcarbon atoms is preferably from 2 to 40. Specific examples thereof mayinclude vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl,1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1-butenyl, 1,3-butadienyl,allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl,2-phenyl-2-(naphthyl-l-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl,a stilbenyl group, a styrenyl group and the like, but are not limitedthereto.

When the aryl group is a monocyclic aryl group in the presentspecification, the number of carbon atoms is not particularly limited,but is preferably from 6 to 25. Specific examples of the monocyclic arylgroup may include a phenyl group, a biphenyl group, a terphenyl groupand the like, but are not limited thereto.

When the aryl group is a polycyclic aryl group in the presentspecification, the number of carbon atoms is not particularly limited,but is preferably from 10 to 24. Specific examples of the polycyclicaryl group may include a naphthyl group, an anthracenyl group, aphenanthryl group, a pyrenyl group, a perylenyl group, a chrysenylgroup, a fluorenyl group and the like, but are not limited thereto.

In the present specification, the fluorenyl group may be substituted,and adjacent substituents may bond to each other to form a ring.

When the fluorenyl group is substituted,

and the like may be included. However, the structure is not limitedthereto.

In the present specification, the heterocyclic group is a groupincluding one or more atoms that are not carbon, that is, heteroatoms,and specifically, the heteroatom may include one or more atoms selectedfrom the group consisting of O, N, Se, S and the like. The number ofcarbon atoms of the heterocyclic group is not particularly limited, butis preferably from 2 to 60. Examples of the heterocyclic group mayinclude a thiophene group, a furan group, a pyrrole group, an imidazolegroup, a thiazole group, an oxazole group, an oxadiazole group, atriazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, atriazine group, a triazole group, an acridyl group, a pyridazine group,a pyrazinyl group, a qinolinyl group, a quinazoline group, aquinoxalinyl group, a phthalazinyl group, a pyridopyrimidinyl group, apyridopyrazinyl group, a pyrazinopyrazinyl group, an isoquinoline group,an indole group, a carbazole group, a benzoxazole group, a benzimidazolegroup, a benzothiazole group, a benzocarbazole group, a benzothiophenegroup, a dibenzothiophene group, a benzofuranyl group, a phenanthridylgroup, a phenanthroline group, a thiazolyl group, an isoxazolyl group,an oxadiazolyl group, a thiadiazolyl group, a benzothiazolyl group, aphenothiazinyl group, a dibenzofuranyl group and the like, but are notlimited thereto.

In the present specification, the number of carbon atoms of the aminegroup is not particularly limited, but is preferably from 1 to 30. Inthe amine group, the N atom may be substituted with an aryl group, analkyl group, an arylalkyl group, a heterocyclic group and the like, andspecific examples of the amine group may include a methylamine group, adimethylamine group, an ethylamine group, a diethylamine group, aphenylamine group, a naphthylamine group, a biphenylamine group, ananthracenylamine group, a 9-methyl-anthracenylamine group, adiphenylamine group, a phenylnaphthylamine group, a ditolylamine group,a phenyltolylamine group, a triphenylamine group and the like, but arenot limited thereto.

In the present specification, the aryl group in the aryloxy group, thearylthio group and the arylsulfoxy group is the same as the examples ofthe aryl group described above. Specific examples of the aryloxy groupmay include phenoxy, p-tolyloxy, m-tolyloxy, 3,5-dimethyl-phenoxy,2,4,6-trimethylphenoxy, p-tert-butylphenoxy, 3-biphenyloxy,4-biphenyloxy, 1-naphthyloxy, 2-naphthyloxy, 4-methyl-1-naphthyloxy,5-methyl-2-naphthyloxy, 1-anthryloxy, 2-anthryloxy, 9-anthryloxy,1-phenanthryloxy, 3-phenanthryloxy, 9-phenanthryloxy, benzyloxy,p-methylbenzyloxy and the like, examples of the arylthio group mayinclude a phenylthio group, a 2-methylphenylthio group, a4-tert-butylphenylthio group and the like, and examples of thearylsulfoxy group may include a benzenesulfoxy group, p-toluenesulfoxygroup and the like, however, the aryloxy group, the arylthio group andthe arylsulfoxy group are not limited thereto.

In the present specification, the alkyl group in the alkylthio group andthe alkylsulfoxy group is the same as the examples of the alkyl groupdescribed above. Specific examples of the alkylsulfoxy group may includea methylsulfoxy group, an ethylsulfoxy group, a propylsulfoxy group, abutylsulfoxy group and the like, but are not limited thereto.

In the present specification, the alkylthio group means a substituentrepresented by —S—R (R is an alkyl group), and may be linear, branchedor cyclic. The number of carbon atoms of the alkylthio group is notparticularly limited, but is preferably from 1 to 20. Specific examplesthereof may include methylthio, ethylthio, n-propylthio, isopropylthio,i-propylthio, n-butylthio, isobutylthio, tert-butylthio, sec-butylthio,n-pentylthio, neopentylthio, isopentylthio, n-hexylthio,3,3-dimethylbutylthio, 2-ethylbutylthio, n-octylthio, n-nonylthio,n-decylthio, benzylthio, p-methylbenzylthio and the like, but are notlimited thereto.

In the present specification, the heteroring may be cycloheteroalkyl,cycloheteroalkenyl, cycloheteroketone, an aliphatic heteroring, anaromatic heteroring or a fused ring thereof, and may be selected fromamong the examples of the heterocyclic group except for those that arenot monovalent.

According to one embodiment of the present specification, in ChemicalFormula 1, X1 is S.

According to one embodiment of the present specification, in ChemicalFormula 1, X2 is S.

According to one embodiment of the present specification, in ChemicalFormula 1, X1 is O.

According to one embodiment of the present specification, in ChemicalFormula 1, X2 is O.

According to one embodiment of the present specification, in ChemicalFormula 1, Y1 is CR″.

According to one embodiment of the present specification, in ChemicalFormula 1, Y2 is CR″.

According to one embodiment of the present specification, in ChemicalFormula 1, R1 is hydrogen.

According to one embodiment of the present specification, in ChemicalFormula 1, R2 is hydrogen.

According to one embodiment of the present specification, the first unitis represented by the following Chemical Formula 1-1.

[Chemical Formula 1-1]

In Chemical Formula 1-1,

R1 and R2 have the same definitions as in Chemical Formula 1, and

R11 and R12 are the same as or different from each other, and eachindependently a substituted or unsubstituted alkyl group; a substitutedor unsubstituted alkoxy group; a substituted or unsubstituted aryloxygroup; a substituted or unsubstituted alkylthio group; a substituted orunsubstituted arylthio group; a substituted or unsubstituted aryl group;or a substituted or unsubstituted heterocyclic group.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R11 is a substituted or unsubstituted linear or branchedalkoxy group; a substituted or unsubstituted aryl group; or asubstituted or unsubstituted heterocyclic group.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R11 is a linear or branched alkoxy group; an aryl groupsubstituted with a linear or branched alkoxy group; or a heterocyclicgroup substituted with one or more selected from among a linear orbranched alkyl group, a linear or branched alkylthio group, and ahalogen group.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R11 is linear or branched alkoxy group; a phenyl groupsubstituted with a linear or branched alkoxy group; a thiophene groupsubstituted with one or more selected from among a linear or branchedalkyl group, a linear or branched alkylthio group, and a halogen group ;or a benzothiophene group substituted with a linear or branched allcylgroup.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R12 is a substituted or unsubstituted linear or branchedalkoxy group; a substituted or unsubstituted aryl group; or asubstituted or unsubstituted heterocyclic group.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R12 is a linear or branched alkoxy group; an aryl groupsubstituted with a linear or branched alkoxy group; or a heterocyclicgroup substituted with one or more selected from among a linear orbranched alkyl group, a linear or branched alkylthio group, and ahalogen group.

According to one embodiment of the present specification, in ChemicalFormula 1-1, R12 is a linear or branched alkoxy group; a phenyl groupsubstituted with a linear or branched alkoxy group; a thiophene groupsubstituted with one or more selected from among a linear or branchedalkyl group, a linear or branched alkylthio group, and a halogen group;or a benzothiophene group substituted with a linear or branched alkylgroup.

According to one embodiment of the present specification, the first unitis represented by any one of the following Chemical Formulae 1-2 to 1-7.

In Chemical Formulae 1-2 to 1-7,

A3 and A4 are the same as or different from each other, and eachindependently a halogen group,

R111, R112, R211 and R212 are the same as or different from each other,and each independently a substituted or unsubstituted alkyl group; asubstituted or unsubstituted silyl group; or a substituted orunsubstituted alkylthio group, and

R311, R312, R411 and R412 are the same as or different from each other,and each independently a substituted or unsubstituted alkyl group; or asubstituted or unsubstituted alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R111 is a substituted or unsubstituted linear orbranched alkyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R111 is a linear or branched alkyl group.According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6,

R111 is a branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R111 is a 2-ethylhexyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R112 is a substituted or unsubstituted linear orbranched alkyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R112 is a linear or branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R112 is a branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, R112 is a 2-ethylhexyl group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R211 is a substituted or unsubstituted linear or branchedalkyl group; a silyl group unsubstituted or substituted with an alkylgroup or an aryl group; or a substituted or unsubstituted linear orbranched alkylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R211 is a linear or branched alkyl group; a silyl groupunsubstituted or substituted with a linear alkyl group or an aryl group;or a linear or branched alkylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R211 is a branched alkyl group; a silyl group substitutedwith a linear alkyl group; or a branched alkylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R211 is a 2-ethylhexyl group; a tributylsilyl group; or a2-ethylhexylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R212 is a substituted or unsubstituted linear or branchedalkyl group; a silyl group unsubstituted or substituted with an alkylgroup; or a substituted or unsubstituted linear or branched alkylthiogroup.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R212 is a linear or branched alkyl group; a silyl groupunsubstituted or substituted with a linear alkyl group; or a linear orbranched alkylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R212 is a branched alkyl group; a silyl group substitutedwith a linear alkyl group; or a branched alkylthio group.

According to one embodiment of the present specification, in ChemicalFormula 1-3, R212 is a 2-ethylhexyl group; a tributylsilyl group; or a2-ethylhexylthio group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R311 is a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R311 is a linear or branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R311 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R311 is a 2-ethylhexyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R312 is a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R312 is a linear or branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R312 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 1-4 and 1-5, R312 is a 2-ethylhexyloxy group.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a substituted or unsubstituted alkylgroup.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a substituted or unsubstitutedlinear or branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a branched C₆-C₁₅ alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a branched C₈-C₁₂ alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 1-7, R411 and R412 are each a 2-butyloctyl group.

According to one embodiment of the present specification, in ChemicalFormulae 1-2 and 1-6, A3 and A4 are each fluorine or chlorine.

According to one embodiment of the present specification, in ChemicalFormula 2, X3 is S.

According to one embodiment of the present specification, in ChemicalFormula 2, X4 is S.

According to one embodiment of the present specification, the secondunit is represented by the following Chemical Formula 2-1.

In Chemical Formula 2-1,

R3 to R6, A1 and A2 have the same definitions as in Chemical Formula 2.

According to one embodiment of the present specification, in ChemicalFormula 2, R3 to R6 are hydrogen.

According to one embodiment of the present specification, in ChemicalFormula 2, A1 and A2 are fluorine.

According to one embodiment of the present specification, the secondunit is represented by the following Chemical Formula 2-2.

According to one embodiment of the present specification, in ChemicalFormula 3, Cy is a heteroring including one or more of N, O, S, Si, Ge,Te, P and Se as a heteroatom, and substituted or unsubstituted.

According to one embodiment of the present specification, in ChemicalFormula 3, Cy is a monocyclic 5-membered or 6-membered heteroringincluding one or more of N, O, S, Si, Ge, Te, P and Se as a heteroatom,and substituted or unsubstituted.

According to one embodiment of the present specification, the third unitis represented by the following Chemical Formula 3-1 or 3-2.

In Chemical Formulae 3-1 and 3-2,

R7 and R8 have the same definitions as in Chemical Formula 3,

X7 is CRR′, NR, O, SiRR′, PR, S, GeRR′, Se or Te,

Y3 to Y6 are the same as or different from each other, and eachindependently CR″, N, SiR″, P or GeR″,

R., R′, R″, R9 and R10 are the same as or different from each other, andeach independently hydrogen; a substituted or unsubstituted alkyl group;a substituted or unsubstituted alkoxy group; a substituted orunsubstituted aryloxy group; a substituted or unsubstituted alkylthiogroup; a substituted or unsubstituted arylthio group; a substituted orunsubstituted aryl group; or a substituted or unsubstituted heterocyclicgroup.

According to one embodiment of the present specification, in ChemicalFormula 4, X5 is S.

According to one embodiment of the present specification, in ChemicalFormula 4, X6 is NR.

According to one embodiment of the present specification, in ChemicalFormula 4, Q1 and Q2 are O.

According to one embodiment of the present specification, the third unitis represented by any one of the following Chemical Formulae 3-3 to 3-7.

In Chemical Formulae 3-3 to 3-7,

R7 and R8 have the same definitions as in Chemical Formula 3,

R9, R10 and R19 are the same as or different from each other, and eachindependently hydrogen; a substituted or unsubstituted alkyl group; asubstituted or unsubstituted alkoxy group; a substituted orunsubstituted aryloxy group; a substituted or unsubstituted alkylthiogroup; a substituted or unsubstituted arylthio group; a substituted orunsubstituted aryl group; or a substituted or unsubstituted heterocyclicgroup.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a substituted or unsubstituted alkoxygroup.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a linear or branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a linear alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a linear C₁-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or a linear C₁₀-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is hydrogen; or an n-dodecyloxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is a C₃-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is a C₁₀-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R7 is a 2-butyloctyloxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a substituted or unsubstituted alkoxygroup.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a linear or branched alkoxy group.According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a linear alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a linear C₁-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or a linear C₁₀-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is hydrogen; or an n-dodecyloxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is a C₃-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is a C₁₀-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3, R8 is a 2-butyloctyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a substituted or unsubstituted alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a linear or branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a linear alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is hydrogen; or a linear C₁-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is hydrogen; or a linear C₁₀-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is an n-dodecyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a C₃-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a C₁₀-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R7 is a 2-butyloctyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a substituted or unsubstituted alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a substituted or unsubstituted linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a linear or branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a linear alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is hydrogen; or a linear C_(i)-C₂₀ alkoxygroup.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is hydrogen; or a linear C₁₀-C₂₀ alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is an n-dodecyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a C₃-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a C₁₀-C₂₀ branched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-3 and 3-4, R8 is a 2-butyloctyloxy group.

According to one embodiment of the present specification, in ChemicalFormulae 3-5 and 3-6, R7 and R8 are hydrogen.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a substituted or unsubstituted alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a substituted or unsubstituted linear or branchedalkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a branched C₆-C₁₅ alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a branched C₈-C₁₂, alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-5, R19 is a 2-ethylhexyl group or a 2-butyloctyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-6, R9 and R10 are the same as or different from each other,and each independently a substituted or unsubstituted aryl group.

According to one embodiment of the present specification, in ChemicalFormula 3-6, R9 and R10 are the same as or different from each other,and each independently an aryl group substituted with a linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3-6, R9 and R10 are the same as or different from each other,and each independently a phenyl group substituted with a linear orbranched alkoxy group.

According to one embodiment of the present specification, in ChemicalFormula 3-6, R9 and R10 are the same as or different from each other,and each independently a phenyl group substituted with a linear alkoxygroup.

According to one embodiment of the present specification, in ChemicalFormula 3-6, R9 and R10 are a phenyl group substituted with ann-octyloxy group.

According to one embodiment of the present specification, in ChemicalFormula 3-7, R19 is a substituted or unsubstituted alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-7, R19 is a substituted or unsubstituted linear or branchedalkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-7, R19 is a branched alkyl group.

According to one embodiment of the present specification, in ChemicalFormula 3-7, R19 is a 2-ethylhexyl group.

According to one embodiment of the present specification, the polymerincludes a unit represented by the following Chemical Formula 5.

[Chemical Formula 5]

In Chemical Formula 5,

l is, as a mole fraction, a real number of 0<l<1,

m is, as a mole fraction, a real number of 0<m<1,

l+m=1,

A is the first unit represented by Chemical Formula 1,

B is the second unit represented by Chemical Formula 2,

C and C′ are the same as or different from each other, and eachindependently the third unit represented by Chemical Formula 3 orChemical Formula 4, and

n is, as a repetition number of the unit, an integer of 1 to 10,000.

A1 and A2 in the second unit represented by Chemical Formula 2-1 of thepresent specification, and an S atom of thiophene; or A1 and A2 in thesecond unit represented by Chemical Formula 2-1, and an S atom of thefirst unit represented by Chemical Formula 1-1 interact with each other.

Herein, interacting with each other means a chemical structure or atomsforming a chemical structure having non-covalent bonding interactionsthat influence each other by an action other than covalent bonds, andfor example, may mean chalcogen bonds.

In addition, by the third unit represented by any one of ChemicalFormulae 3-3 to 3-7 including R7 and R8 in one embodiment of the presentspecification, an O atom of R7 and R8; A1 and A2 of the second unitrepresented by Chemical Formula 2; and an S atom of the first unitrepresented by

Chemical Formula 1 may interact with each other to form a planarstructure.

Accordingly, an increase in the current may be induced when includingthe polymer according to one embodiment of the present specification,and a device with high efficiency may be provided.

According to one embodiment of the present specification, A is the firstunit represented by Chemical Formula 1-1.

According to one embodiment of the present specification, B is thesecond unit represented by Chemical Formula 2-1.

According to one embodiment of the present specification, C is the thirdunit represented by any one selected from among Chemical Formulae 3-3 to3-7.

According to one embodiment of the present specification, C′ is thethird unit represented by any one selected from among Chemical Formulae3-3 to 3-7.

According to one embodiment of the present specification, the polymerincludes a unit represented by the following Chemical Formula 5-1 or5-2.

In Chemical Formulae 5-1 and 5-2,

X1 to X6, Y1, Y2, R1 to R8, Cyl, Q1, Q2, A1 and A2 have the samedefinitions as in Chemical Formulae 1 to 4,

Cy11 is a substituted or unsubstituted heteroring,

Q11 and Q12 are the same as or different from each other, and eachindependently O or S,

X15 and X16 are the same as or different from each other, and eachindependently CRR′, NR, O, SiRR′, PR, S, GeRR′, Se or Te,

R, R′, R17 and R18 are the same as or different from each other, andeach independently hydrogen; deuterium; a halogen group; a nitrilegroup; a nitro group; an imide group; an amide group; a hydroxyl group;a substituted or unsubstituted alkyl group; a substituted orunsubstituted cycloalkyl group; a substituted or unsubstituted alkoxygroup; a substituted or unsubstituted aryloxy group; a substituted orunsubstituted alkylthio group; a substituted or unsubstituted arylthiogroup; a substituted or unsubstituted alkylsulfoxy group; a substitutedor unsubstituted arylsulfoxy group; a substituted or unsubstitutedalkenyl group; a substituted or unsubstituted amine group; a substitutedor unsubstituted aryl group; or a substituted or unsubstitutedheterocyclic group,

l is, as a mole fraction, a real number of 0<l<1,

m is, as a mole fraction, a real number of 0<m<1,

l+m=1, and

n is, as a repetition number of the unit, an integer of 1 to 10,000.

According to one embodiment of the present specification, the polymerincludes a unit represented by any one of the following ChemicalFormulae 5-3-1 to 5-3-3.

In Chemical Formulae 5-3-1 to 5-3-3,

A1 to A4 are the same as or different from each other, and eachindependently a halogen group,

R107, R108, R207 and R208 are the same as or different from each other,and each independently a substituted or unsubstituted alkoxy group,

R111, R112, R211 and R212 are the same as or different from each other,and each independently a substituted or unsubstituted alkyl group; asubstituted or unsubstituted silyl group; or a substituted orunsubstituted alkylthio group,

R411 and R412 are the same as or different from each other, and eachindependently a substituted or unsubstituted alkyl group; or asubstituted or unsubstituted alkoxy group,

l is, as a mole fraction, a real number of 0<l<1,

m is, as a mole fraction, a real number of 0<m<1,

l+m=1, and

n is, as a repetition number of the unit, an integer of 1 to 10,000.

According to one embodiment of the present specification, the polymerincludes a unit represented by any one of the following ChemicalFormulae 5-4 to 5-60.

In Chemical Formulae 5-4 to 5-60,

l is, as a mole fraction, a real number of 0<l<1,

m is, as a mole fraction, a real number of 0<m<1,

l+m=1, and

n is, as a repetition number of the unit, an integer of 1 to 10,000.

In one embodiment of the present specification, 1 is 0.5.

In another embodiment, m is 0.5.

In another embodiment of the present specification, 1 is 0.75.

In one embodiment of the present specification, m is 0.25.

In one embodiment of the present specification, the polymer is a randompolymer. In addition, the random polymer has enhanced solubility, whichis economically effective in terms of time and costs in a devicemanufacturing process.

In one embodiment of the present specification, an end group of thepolymer is a substituted or unsubstituted heterocyclic group or asubstituted or unsubstituted aryl group.

In one embodiment of the present specification, an end group of thepolymer is a heterocyclic group unsubstituted or substituted with ahalogen group, an alkyl group or a haloalkyl group; or an aryl groupunsubstituted or substituted with a halogen group, an alkyl group or ahaloalkyl group.

In one embodiment of the present specification, an end group of thepolymer is a heterocyclic group unsubstituted or substituted with ahalogen group, a C₁-C₆ alkyl group or a C₁-C₆ fluoroalkyl group; or anaryl group unsubstituted or substituted with a halogen group, a C₁-C₆alkyl group or a C₁-C₆ haloalkyl group. In one embodiment of the presentspecification, an end group of the polymer is a4-(trifluoromethyl)phenyl group.

In one embodiment of the present specification, an end group of thepolymer is a bromo-thiophene group.

In another embodiment, an end group of the polymer may be atrifluoro-benzene group.

According to another embodiment of the present specification, thepolymer may not have an end group. In other words, the polymer may be apolymer that does not have end capping.

According to one embodiment of the present specification, the polymerpreferably has a number average molecular weight of 5,000 g/mol to1,000,000 g/mol.

According to one embodiment of the present specification, the polymermay have molecular weight distribution of 1 to 10. Preferably, thepolymer has molecular weight distribution of 1 to 3.

As the molecular weight distribution decreases and the number averagemolecular weight increases, favorable electrical properties andmechanical properties are obtained.

In addition, the number average molecular weight is preferably 100,000g/mol or less so as to have solubility at a certain level or higher,which is advantageous in using a solution coating method.

As for the molecular weight, the number average molecular weight (Mn)and the weight average molecular weight (Mw) are measured by GPC usingchlorobenzene as a solvent, and the molecular weight distribution meansa number dividing the weight average molecular weight (Mw) by the numberaverage molecular weight (Mn), that is, weight average molecular weight(Mw)/number average molecular weight (Mn).

The polymer may be prepared based on preparation examples to describebelow. A monomer of each unit of the polymer is introduced together withPd₂(dba)₃ and P(o-tolyl)₃ using chlorobenzene as a solvent, and thepolymer is prepared through polymerization using a microwave reactor.

The polymer according to the present specification may be prepared usinga multi-step chemical reaction. After preparing monomers through analkylation reaction, a Grignard reaction, a Suzuki coupling reaction, aStille coupling reaction and the like, final polymers may be preparedthrough a carbon-carbon coupling reaction such as a Stille couplingreaction. When a substituent to introduce is a boronic acid or a boronicester compound, a Suzuki coupling reaction may be used, and when asubstituent to introduce is a tributyltin or trimethyltin compound, aStille coupling reaction may be used, however, the method is not limitedthereto.

In one embodiment of the present specification, the non-fullerene-basedelectron acceptor is represented by the following Chemical Formula A:

In Chemical Formula A,

R201 to R204 are the same as or different from each other, and eachindependently a substituted or unsubstituted aryl group; or asubstituted or unsubstituted heteroaryl group,

A101 to A108 are the same as or different from each other, and eachindependently hydrogen; a halogen group; or a substituted orunsubstituted alkyl group.

According to one embodiment of the present specification, in ChemicalFormula A, R201 to R204 are the same as or different from each other,and each independently an aryl group unsubstituted or substituted withan allcyl group; or a heteroaryl group unsubstituted or substituted withan alkyl group.

According to one embodiment of the present specification, in ChemicalFormula A, R201 to R204 are the same as or different from each other,and each independently a phenyl group unsubstituted or substituted withan alkyl group; or a thiophene group unsubstituted or substituted withan alkyl group.

According to one embodiment of the present specification, in ChemicalFormula A, R201 to R204 are the same as or different from each other,and each independently a phenyl group substituted with an n-hexyl group;or a thiophene group substituted with an n-hexyl group.

According to one embodiment of the present specification, in ChemicalFormula A, R201 to R204 are a phenyl group substituted with an n-hexylgroup.

According to one embodiment of the present specification, in ChemicalFormula A, R201 to R204 are a thiophene group substituted with ann-hexyl group.

According to one embodiment of the present specification, in ChemicalFormula A, A101 to A108 are hydrogen; fluorine; or a linear or branchedalkyl group.

According to one embodiment of the present specification, in ChemicalFormula A, A101 to A104 are the same as or different from each other,and each independently hydrogen; fluorine; or a linear alkyl group.

According to one embodiment of the present specification, in ChemicalFormula A, A101 to A104 are the same as or different from each other,and each independently hydrogen; fluorine; or a methyl group.

According to one embodiment of the present specification, ChemicalFormula A is represented by any one of the following Chemical FormulaeA-1 to A-5.

In one embodiment of the present specification, the electron donor andthe electron acceptor form a bulk heterojunction (BHJ). The bulkheterojunction means an electron donor material and an electron acceptormaterial being mixed together in a photoactive layer of an organic solarcell.

In one embodiment of the present specification, the electron donor mayinclude additional electron donor compounds or polymers in addition tothe above-described polymer, or may be formed only with theabove-described polymer. In one embodiment of the present specification,the electron donor and the electron acceptor may be included in a massratio of 2:1 to 1:4, and preferably in a mass ratio of 1:1 to 1:4.

In one embodiment of the present specification, the composition for anorganic material layer of an organic solar cell further includes anadditive.

In one embodiment of the present specification, the additive has amolecular weight of 50 g/mol to 500 g/mol.

In another embodiment, the additive is an organic material having aboiling point of 30° C. to 300° C.

In the present specification, the organic material means a materialincluding at least one or more carbon atoms.

In one embodiment, the additive may further include one or two types ofadditives among additives selected from the group consisting of1,8-diiodooctane (DIO), 1-chloronaphthalene (1-CN), diphenyl ether(DPE), octanedithiol and tetrabromothiophene.

The additive may be included in 0.1 v/v % to 5 v/v % and specifically in0.3 v/v % to 0.8 v/v % with respect to the total volume of thecomposition or a photoactive layer of an organic solar cell to describelater.

One embodiment of the present specification provides an organic solarcell including a first electrode; a second electrode disposed oppositeto the first electrode; and one or more organic material layers disposedbetween the first electrode and the second electrode and including aphotoactive layer, wherein one or more layers of the organic materiallayers include the composition for an organic material layer of anorganic solar cell according to the above-described embodiments.

In the present specification, a description of one member being placed“on” another member includes not only a case of the one member adjoiningthe another member but a case of still another member being presentbetween the two members.

The organic solar cell according to one embodiment of the presentspecification includes a first electrode, a photoactive layer and asecond electrode. Herein, the photoactive layer may include thecomposition for an organic material layer of an organic solar cellaccording to the above-described embodiments. The organic solar cell mayfurther include a substrate, a hole transfer layer and/or an electrontransfer layer.

In one embodiment of the present specification, when the organic solarcell receives photons from an external light source, excitons areseparated into electrons and holes at an interface of an electron donorand an electron acceptor. The separated holes are transferred to ananode from a photoactive layer after passing through a hole transferlayer through the electron donor, and the separated electrons aretransferred to a cathode from a photoactive layer after passing throughan electron transfer layer through the electron acceptor.

In one embodiment of the present specification, the organic materiallayer includes a hole transfer layer, a hole injection layer, or a layercarrying out hole transfer and hole injection at the same time, and thehole transfer layer, the hole injection layer, or the layer carrying outhole transfer and hole injection at the same time includes the polymer.

In another embodiment, the organic material layer includes an electroninjection layer, an electron transfer layer, or a layer carrying outelectron injection and electron transfer at the same time, and theelectron injection layer, the electron transfer layer, or the layercarrying out electron injection and electron transfer at the same timeincludes the polymer.

FIG. 1 is a diagram illustrating the organic solar cell according to oneembodiment of the present specification, which has structure in which anelectron transfer layer (102), a photoactive layer (103), a holetransfer layer (104) and a second electrode (105) are consecutivelylaminated on a first electrode (101), however, the structure of theorganic solar cell of the present specification is not limited thereto.

In one embodiment of the present specification, the organic solar cellmay further include additional organic material layers. The organicsolar cell may reduce the number of organic material layers by using anorganic material having various functions at the same time. In oneembodiment of the present specification, the first electrode is ananode, and the second electrode is a cathode. In another embodiment, thefirst electrode is a cathode, and the second electrode is an anode.

In one embodiment of the present specification, the organic solar cellmay have a structure in which a cathode, a photoactive layer and ananode are arranged in consecutive order, or may have a structure inwhich an anode, a photoactive layer and a cathode are arranged inconsecutive order, however, the structure is not limited thereto.

In another embodiment, the organic solar cell may have a structure inwhich an anode, a hole transfer layer, a photoactive layer, an electrontransfer layer and a cathode are arranged in consecutive order, or mayhave a structure in which a cathode, an electron transfer layer, aphotoactive layer, a hole transfer layer and an anode are arranged inconsecutive order, however, the structure is not limited thereto.

In one embodiment of the present specification, the organic solar cellhas a normal structure. The normal structure may be forming an anode ona substrate. Specifically, according to one embodiment of the presentspecification, the first electrode formed on the substrate may be ananode when the organic solar cell has a normal structure.

In one embodiment of the present specification, the organic solar cellhas an inverted structure. The inverted structure may mean forming acathode on a substrate. Specifically, according to one embodiment of thepresent specification, the first electrode formed on the substrate maybe a cathode when the organic solar cell has an inverted structure.

In one embodiment of the present specification, the organic solar cellhas a tandem structure. In this case, the organic solar cell may includetwo or more photoactive layers. The organic solar cell according to oneembodiment of the present specification may have the photoactive layerin one, two or more layers.

In another embodiment, a buffer layer may be disposed between thephotoactive layer and the hole transfer layer or between the photoactivelayer and the electron transfer layer. Herein, a hole injection layermay be further disposed between the anode and the hole transfer layer.In addition, an electron injection layer may be further disposed betweenthe cathode and the electron transfer layer. The substrate in thepresent specification may include a glass substrate or a transparentplastic substrate having excellent transparency, surface smoothness,handling easiness and water resistance, but is not limited thereto, andsubstrates commonly used in organic solar cells may be used withoutlimit. Specific examples thereof include glass, polyethyleneterphthalate (PET), polyethylene naphthalate (PEN), polypropylene (PP),polyimide (PI), triacetyl cellulose (TAC) and the like, but are notlimited thereto.

The first electrode may include a material that is transparent and hasexcellent conductivity, but is not limited thereto. Examples of thefirst electrode material include metals such as vanadium, chromium,copper, zinc or gold, or alloys thereof; metal oxides such as zincoxides, indium oxides, indium tin oxides (ITO) or indium zinc oxides(IZO); combinations of metals and oxides such as ZnO:Al or SnO₂:Sb;conductive polymers such as poly(3-methylthiophene),poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole andpolyaniline, and the like, but are not limited thereto.

A method of forming the first electrode is not particularly limited,however, the first electrode may be formed by being applied to onesurface of a substrate or coated in the form of a film using a methodsuch as sputtering, E-beam, thermal deposition, spin coating, screenprinting, inkjet printing, doctor blade or gravure printing.

When the first electrode is formed on a substrate, the result may gothrough processes of cleaning, moisture removal and modifying to behydrophilic.

For example, after a patterned ITO substrate is cleaned with a cleaningagent, acetone and isopropyl alcohol (IPA) in consecutive order, the ITOsubstrate is dried for 1 minute to 30 minutes at 100° C. to 150° C.,preferably for 10 minutes at 120° C., on a heating plate in order toremove moisture, and when the substrate is completely cleaned, thesubstrate surface is modified to be hydrophilic.

Through the surface modification such as above, the junctional surfacepotential may be maintained at a level suitable for the surfacepotential of the photoactive layer. In addition, when the surface ismodified, a polymer thin film may be readily formed on the firstelectrode, and the quality of the thin film may be improved.

Preprocessing technologies of the first electrode include a) a surfaceoxidation method using parallel plate discharge, b) a method ofoxidizing the surface through ozone generated by UV rays under a vacuum,and c) an oxidation method using the oxygen radicals generated byplasma.

One of the methods described above may be selected depending on thecondition of the first electrode or the substrate. However, it iscommonly preferred to prevent the leave of oxygen on the surface of thefirst electrode or the substrate and to suppress the remaining ofmoisture and organic materials as much as possible, no matter whichmethod is used. In this case, practical effects of the preprocessing maybe maximized.

As a specific example, a method of oxidizing the surface through ozonegenerated by UV rays may be used. Herein, the patterned ITO substratemay be fully dried by baking the patterned ITO substrate on a hot plateafter ultrasonic cleaning, and the patterned ITO substrate is introducedinto a chamber and then may be cleaned by ozone generated by reactingoxygen gas with UV light using a UV lamp.

However, the method of surface modification of the patterned ITOsubstrate in the present specification is not particularly limited, andany method oxidizing a substrate may be used.

The second electrode may include a metal having small work function, butis not limited thereto. Specific examples thereof may include metalssuch as magnesium, calcium, sodium, potassium, titanium, indium,yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloysthereof; or multilayer structure materials such as LiF/Al, LiO₂/Al,LiF/Fe, Al:Li, Al:BaF₂ and Al:BaF₂:Ba, but are not limited thereto.

The second electrode may be formed by being deposited inside a thermaldeposition apparatus having a degree of vacuum of 5×10⁻⁷ torr or less,however, the formation is not limited to this method.

The hole transfer layer and/or the electron transfer layer material playa role of efficiently transferring the electrons and the holes separatedin the photoactive layer to an electrode, and the material is notparticularly limited.

The hole transfer layer material may includepoly(3,4-ethylenedioxythiophene) doped with poly(styrenesulfonic acid)(PEDOT:PSS), molybdenum oxides (MoO_(x)); vanadium oxide (V₂O₅); nickeloxide (NiO); tungsten oxides (WO_(x)), and the like, but is not limitedthereto.

The electron transfer layer material may include electron-extractingmetal oxides, and may specifically include a metal complex of8-hydroxyquinoline; a complex including Alq₃; a metal complex includingLiq; LiF; Ca; titanium oxides (TiO_(x)); zinc oxide (ZnO); cesiumcarbonate (Cs₂CO₃), and the like, but is not limited thereto.

The photoactive layer may be formed by dissolving a compositionincluding an electron donor and an electron acceptor in an organicsolvent, and then coating the solution using a method such as spincoating, dip coating, screen printing, spray coating, doctor blade andbrush painting, however, the method is not limited thereto. Hereinafter,the present specification will be described in detail with reference toexamples in order to specifically describe the present specification.However, examples according to the present specification may be modifiedto various other forms, and the scope of the present specification isnot construed as being limited to the examples described below. Examplesof the present specification are provided in order to more fullydescribe the present specification to those having average knowledge inthe art.

[Synthesis of Polymer]

SYNTHESIS EXAMPLE 1

Monomers A-1, B-1 and C-1 were introduced together with Pd₂(dba)₃ andP(o-tolyl)₃ using chlorobenzene as a solvent, and polymerized using amicrowave reactor to prepare the following Polymer 1.

SYNTHESIS EXAMPLE 2

The following Polymer 2 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-2 was used instead ofMonomer A-1.

SYNTHESIS EXAMPLE 3

The following Polymer 3 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer C-2 was used instead ofMonomer C-1.

SYNTHESIS EXAMPLE 4

The following Polymer 4 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-2 was used instead ofMonomer A-1, and the following Monomer C-2 was used instead of MonomerC-1.

SYNTHESIS EXAMPLE 5

The following Polymer 5 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-3 was used instead ofMonomer A-1. A UV-Vis spectrum of Polymer 5 in a film state is shown inFIG. 2.

SYNTHESIS EXAMPLE 6

The following Polymer 6 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-4 was used instead ofMonomer A-1.

SYNTHESIS EXAMPLE 7

The following Polymer 7 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer C-3 was used instead ofMonomer C-1.

SYNTHESIS EXAMPLE 8

The following Polymer 8 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-2 was used instead ofMonomer A-1, and the following Monomer C-3 was used instead of MonomerC-1.

SYNTHESIS EXAMPLE 9

The following Polymer 9 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-3 was used instead ofMonomer A-1, and the following Monomer C-3 was used instead of MonomerC-1.

SYNTHESIS EXAMPLE 10

The following Polymer 10 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer C-4 was used instead ofMonomer C-1.

SYNTHESIS EXAMPLE 11

The following Polymer 11 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-2 was used instead ofMonomer A-1, and the following Monomer C-4 was used instead of MonomerC-1.

SYNTHESIS EXAMPLE 12

The following Polymer 12 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-3 was used instead ofMonomer A-1, and the following Monomer C-4 was used instead of MonomerC-1.

SYNTHESIS EXAMPLE 13

The following Polymer 13 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-3 was used instead ofMonomer A-1. A UV-Vis spectrum of Polymer 13 in a film state is shown inFIG. 3.

SYNTHESIS EXAMPLE 14

The following Polymer 14 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-4 was used instead ofMonomer A-1.

SYNTHESIS EXAMPLE 15

The following Polymer 15 was prepared in the same manner as in SynthesisExample 1 except that the following Monomer A-5 was used instead ofMonomer A-1.

Molecular weights and molecular weight distribution of the polymersprepared in Synthesis Examples 1 to 15 are shown in the following Table1.

TABLE 1 PDI (Molecular Mn (Number Mw (Weight Weight Average AverageMolecular Distribution, Molecular Weight) Weight) Mw/Mn) Polymer 133,860 57,490 1.7 Polymer 2 62,300 71,900 1.15 Polymer 3 28,500 42,7201.50 Polymer 4 35,870 48,250 1.34 Polymer 5 30,300 59,650 1.97 Polymer 627,850 36,290 1.3 Polymer 7 19,930 28,590 1.43 Polymer 8 20,080 30,2201.50 Polymer 9 25,370 34,290 1.35 Polymer 10 29,930 40,590 1.35 Polymer11 31,220 39,680 1.27 Polymer 12 33,420 42,290 1.26 Polymer 13 30,09058,900 1.96 Polymer 14 29,100 52,250 1.80 Polymer 15 26,088 63,334 2.43

In Table 1, as for the molecular weight, the number average molecularweight (Mn) and the weight average molecular weight (Mw) were measuredby GPC using chlorobenzene as a solvent, and the molecular weightdistribution means a number dividing the weight average molecular weight(Mw) by the number average molecular weight (Mn), that is, weightaverage molecular weight (Mw)/number average molecular weight (Mn).

Only synthesis methods of Polymers 1 to 15 are illustrated above,however, polymers other the above-described polymers may be synthesizedby properly changing substituents of Chemical Formulae 1, 2 and 3, or 1,2 and 4 according to one embodiment of the present specification.

[Manufacture of Organic Solar Cell]

EXAMPLE 1

A composite solution was prepared by dissolving Polymer 1 and thefollowing Chemical Formula A-1 (Solarmer Materials Inc.) inchlorobenzene (CB) in a weight ratio of 1:2. Herein, the concentrationwas adjusted to 2 wt %, and the organic solar cell employed an invertedstructure of ITO/ZnO/photoactive layer/MoO₃/Ag.

Specifically, ITO was formed on a substrate as a first electrode, theITO substrate was ultrasonic cleaned using distilled water, acetone and2-propanol, and the ITO surface was ozone treated for 10 minutes.

On the ITO, ZnO was spin-coated to form an electron transfer layer(thickness 40 nm). Then, the composite solution of Polymer 1 and thefollowing Chemical Formula A-1 was spin-coated on the electron transferlayer to form a photoactive layer (thickness 100 nm), and a holetransfer layer was formed on the photoactive layer by depositing MoO₃ toa thickness of 10 nm. Lastly, for forming a second electrode, Ag wasdeposited to a thickness of 100 nm using a thermal evaporator under avacuum of 3×10⁻⁸ torr, and an organic solar cell was manufactured.

EXAMPLE 2

An organic solar cell was manufactured in the same manner as in Example1 except that the following Chemical Formula A-2 (Solarmer MaterialsInc.) was used instead of Chemical Formula A-1.

EXAMPLE 3

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 2 was used instead of Polymer 1.

EXAMPLE 4

An organic solar cell was manufactured in the same manner as in Example3 except that Chemical Formula A-2 (Solarmer Materials Inc.) was usedinstead of Chemical Formula A-1.

EXAMPLE 5

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 3 was used instead of Polymer 1.

EXAMPLE 6

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 4 was used instead of Polymer 1.

EXAMPLE 7

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 5 was used instead of Polymer 1.

EXAMPLE 8

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 6 was used instead of Polymer 1.

EXAMPLE 9

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 7 was used instead of Polymer 1.

EXAMPLE 10

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 8 was used instead of Polymer 1.

EXAMPLE 11

An organic solar cell was manufactured in the same manner as in Example1 except that

Polymer 9 was used instead of Polymer 1.

EXAMPLE 12

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 10 was used instead of Polymer 1.

EXAMPLE 13

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 11 was used instead of Polymer 1.

EXAMPLE 14

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 12 was used instead of Polymer 1.

EXAMPLE 15

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 13 was used instead of Polymer 1.

EXAMPLE 16

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 14 was used instead of Polymer 1.

EXAMPLE 17

An organic solar cell was manufactured in the same manner as in Example1 except that Polymer 15 was used instead of Polymer 1.

COMPARATIVE EXAMPLE 1

An organic solar cell was manufactured in the same manner as in Example1 except that the following Comparative Polymer 1 was used instead ofPolymer 1.

[Comparative Polymer 1]

(Number average molecular weight (Mn): 67,800, weight average molecularweight (Mw): 101,460)

COMPARATIVE EXAMPLE 2

An organic solar cell was manufactured in the same manner as inComparative Example 1 except that Chemical Formula A-2 was used insteadof Chemical Formula A-1.

COMPARATIVE EXAMPLE 3

An organic solar cell was manufactured in the same manner as in Example1 except that PCBM, a fullerene-based compound, was used instead ofChemical Formula A-1, and a concentration of Polymer 1 and PCBM in thecomposite solution was employed as 4 wt %.

COMPARATIVE EXAMPLE 4

An organic solar cell was manufactured in the same manner as in Example3 except that PCBM, a fullerene-based compound, was used instead ofChemical Formula A-1, and a concentration of Polymer 2 and PCBM in thecomposite solution was employed as 4 wt %.

COMPARATIVE EXAMPLE 5

An organic solar cell was manufactured in the same manner as in Example7 except that PCBM, a fullerene-based compound, was used instead ofChemical Formula A-1, and a concentration of Polymer 5 and PCBM in thecomposite solution was employed as 4 wt %.

COMPARATIVE EXAMPLE 6

An organic solar cell was manufactured in the same manner as in Example8 except that PCBM, a fullerene-based compound, was used instead ofChemical Formula A-1, and a concentration of Polymer 6 and PCBM in thecomposite solution was employed as 4 wt %.

Photoelectric conversion properties of the organic solar cellsmanufactured in Examples 1 to 17 and Comparative Examples 1 to 6 weremeasured under a condition of 100 mW/cm² (AM 1.5), and the results areshown in the following Table 2.

TABLE 2 J_(sc) V_(oc) (mA/ η Donor Acceptor (V) cm²) FF (%) Example 1Polymer 1 Chemical 0.899 14.416 0.646 8.37 Formula A-1 Example 2 Polymer1 Chemical 0.764 15.456 0.643 7.59 Formula A-2 Example 3 Polymer 2Chemical 1.024 13.248 0.616 8.36 Formula A-1 Example 4 Polymer 2Chemical 0.886 13.806 0.686 8.39 Formula A-2 Example 5 Polymer 3Chemical 0.908 13.824 0.646 8.11 Formula A-1 Example 6 Polymer 4Chemical 1.014 13.825 0.57 7.99 Formula A-1 Example 7 Polymer 5 Chemical0.953 14.083 0.594 7.97 Formula A-1 Example 8 Polymer 6 Chemical 0.89713.980 0.638 8.00 Formula A-1 Example 9 Polymer 7 Chemical 0.903 14.0900.626 7.96 Formula A-1 Example 10 Polymer 8 Chemical 1.014 13.852 0.5748.06 Formula A-1 Example 11 Polymer 9 Chemical 0.926 13.464 0.607 7.57Formula A-1 Example 12 Polymer 10 Chemical 0.912 13.716 0.628 7.86Formula A-1 Example 13 Polymer 11 Chemical 1.007 13.110 0.594 7.84Formula A-1 Example 14 Polymer 12 Chemical 0.927 13.550 0.622 7.81Formula A-1 Example 15 Polymer 13 Chemical 0.975 13.579 0.586 7.76Formula A-1 Example 16 Polymer 14 Chemical 0.905 13.439 0.678 8.25Formula A-1 Example 17 Polymer 15 Chemical 1.019 13.213 0.615 8.28Formula A-1 Comparative Comparative Chemical 0.912 12.443 0.632 7.17Example 1 Polymer 1 Formula A-1 Comparative Comparative Chemical 0.74615.864 0.598 7.08 Example 2 Polymer 1 Formula A-2 Comparative Polymer 1PCBM 0.780 10.269 0.57 4.589 Example 3 Comparative Polymer 2 PCBM 0.90510.320 0.49 4.548 Example 4 Comparative Polymer 5 PCBM 0.814 9.822 0.514.062 Example 5 Comparative Polymer 6 PCBM 0.787 9.847 0.56 4.340Example 6

The V_(oc) means an open-circuit voltage, the J_(sc) means ashort-circuit current, the FF means a fill factor, and the η meansenergy conversion efficiency. The open-circuit voltage and theshort-circuit current are respectively an x-axis and a y-axis interceptin the four quadrants of a voltage-current density curve, and as thesetwo values increase, solar cell efficiency is preferably enhanced. Inaddition, the fill factor is a value dividing the rectangle area thatmay be drawn inside the curve by the product of the short-circuitcurrent and the open-circuit voltage. The energy conversion efficiencymay be obtained when these three values are divided by the intensity ofirradiated light, and it is preferred as the value is higher.

In Table 2, the second unit according to one embodiment of the presentspecification includes a structure in which two Fs substitute an orthoposition of the benzene ring, and therefore, the two Fs interact with anS atom of the thiophene of the second unit, and interact with the firstunit and the third unit, which increases polymer planarity, increasingsolubility and having excellent electronic properties. Accordingly, itwas seen that the organic solar cells of Examples 1 to 17 including thesame had a higher current value, and had excellent energy conversionefficiency compared to Comparative Polymer 1 including a structure inwhich two Fs of the second unit substitute a para position of thebenzene ring.

Particularly, Polymers 2 and 14 include a structure in which Y1 and Y2are CR″, and R″ is a halogen group of fluorine or chlorine; and athiophene group substituted with a branched alkyl group of the firstunit of the present specification, and therefore, it was seen that thehalogen atom and S of the thiophene of the first unit, O of the thirdunit, and S of the thiophene and two Fs bonding to an ortho position ofthe benzene ring of the second unit interacted with each other achievingexcellent electrical properties, and efficiency of the organic solarcell including the same was very superior.

In addition, it was identified that the organic solar cells of Examples1 to 17 using a non-fullerene-based compound as an electron acceptor hadsignificantly higher energy conversion efficiency compared to theorganic solar cells of Comparative Examples 3 to 6 using afullerene-based compound. As a result, it was identified that thepolymer according to one embodiment of the present specification hadvery superior efficiency with a non-fullerene-based electron acceptor.

What is claimed is:
 1. A composition for an organic material layer of anorganic solar cell comprising: an electron donor including a polymerincluding a first unit of Chemical Formula 1, a second unit of ChemicalFormula 2, and a third unit of Chemical Formula 3 or Chemical Formula 4;and a non-fullerene-based electron acceptor:

wherein: X1 to X6 are the same as or different from each other, and areeach independently CRR′, NR, O, SiRR′, PR, S, GeRR′, Se or Te; Y1 and Y2are the same as or different from each other, and are each independentlyCR″, N, SiR″, P or GeR″; A1 and A2 are the same as or different fromeach other, and are each independently a halogen group; Cy1 is asubstituted or unsubstituted heteroring; Q1 and Q2 are the same as ordifferent from each other, and are each independently O or S; and R, R′,R″ and R1 to R8 are the same as or different from each other, and areeach independently hydrogen, deuterium, a halogen group, a nitrilegroup, a nitro group, an imide group, an amide group, a hydroxyl group,a substituted or unsubstituted alkyl group, a substituted orunsubstituted cycloalkyl group, a substituted or unsubstituted alkoxygroup, a substituted or unsubstituted aryloxy group, a substituted orunsubstituted alkylthio group, a substituted or unsubstituted arylthiogroup, a substituted or unsubstituted alkylsulfoxy group, a substitutedor unsubstituted arylsulfoxy group, a substituted or unsubstitutedalkenyl group, a substituted or unsubstituted amine group, a substitutedor unsubstituted aryl group, or a substituted or unsubstitutedheterocyclic group.
 2. The composition for an organic material layer ofan organic solar cell of claim 1, wherein the non-fullerene-basedelectron acceptor is a compound of Chemical Formula A:

wherein: R201 to R204 are the same as or different from each other, andare each independently a substituted or unsubstituted aryl group, or asubstituted or unsubstituted heteroaryl group; and A101 to A108 are thesame as or different from each other, and are each independentlyhydrogen, a halogen group, or a substituted or unsubstituted alkylgroup.
 3. The composition for an organic material layer of an organicsolar cell of claim 1, wherein the first unit is a unit of ChemicalFormula 1-1:

wherein: R1 and R2 have the same definitions as in Chemical Formula 1;and R11 and R12 are the same as or different from each other, and areeach independently a substituted or unsubstituted alkyl group, asubstituted or unsubstituted alkoxy group, a substituted orunsubstituted aryloxy group, a substituted or unsubstituted alkylthiogroup, a substituted or unsubstituted arylthio group, a substituted orunsubstituted aryl group, or a substituted or unsubstituted heterocyclicgroup.
 4. The composition for an organic material layer of an organicsolar cell of claim 1, wherein the first unit is a unit of any one ofChemical Formulae 1-2 to 1-7:

wherein: A3 and A4 are the same as or different from each other, and areeach independently a halogen group; R111, R112, R211 and R212 are thesame as or different from each other, and are each independently asubstituted or unsubstituted alkyl group, a substituted or unsubstitutedsilyl group, or a substituted or unsubstituted alkylthio group; andR311, R312, R411 and R412 are the same as or different from each other,and are each independently a substituted or unsubstituted alkyl group ora substituted or unsubstituted alkoxy group.
 5. The composition for anorganic material layer of an organic solar cell of claim 1, wherein thesecond unit is a unit of Chemical Formula 2-1:

wherein R3 to R6, A1 and A2 have the same definitions as in ChemicalFormula
 2. 6. The composition for an organic material layer of anorganic solar cell of claim 1, wherein the third unit is a unit of anyone of Chemical Formulae 3-3 to 3-7:

wherein: R7 and R8 have the same definitions as in Chemical Formula 3;and R9, R10 and R19 are the same as or different from each other, andare each independently hydrogen_(.), a substituted or unsubstitutedalkyl group, a substituted or unsubstituted alkoxy group, a substitutedor unsubstituted aryloxy group, a substituted or unsubstituted alkylthiogroup, a substituted or unsubstituted arylthio group, a substituted orunsubstituted aryl group, or a substituted or unsubstituted heterocyclicgroup.
 7. The composition for an organic material layer of an organicsolar cell of claim 1, wherein the polymer includes a unit of ChemicalFormula 5:

wherein: 1 is a mole fraction and is a real number of 0<l<1; m is a molefraction and is a real number of 0<m<1; l+m=1; A is the first unit ofChemical Formula 1; B is the second unit of Chemical Formula 2; C and C′are the same as or different from each other, and are each independentlythe third unit of Chemical Formula 3 or Chemical Formula 4; and n is arepetition number of the unit and is an integer of 1 to 10,000.
 8. Thecomposition for an organic material layer of an organic solar cell ofclaim 1, wherein the polymer includes a unit of Chemical Formula 5-1 orChemical Formula 5-2:

wherein: X1 to X6, Y1, Y2, R1 to R8, Cy1, Q1, Q2, A1 and A2 have thesame definitions as in Chemical Formulae 1 to 4; Cy11 is a substitutedor unsubstituted heteroring; Q11 and Q12 are the same as or differentfrom each other, and are each independently O or S; X15 and X16 are thesame as or different from each other, and are each independently CRR′,NR, O, SiRR′, PR, S, GeRR′, Se or Te; R, R′, R17 and R18 are the same asor different from each other, and are each independently hydrogen,deuterium, a halogen group, a nitrile group, a nitro group, an imidegroup, an amide group, a hydroxyl group, a substituted or unsubstitutedalkyl group, a substituted or unsubstituted cycloalkyl group, asubstituted or unsubstituted alkoxy group, a substituted orunsubstituted aryloxy group, a substituted or unsubstituted alkylthiogroup, a substituted or unsubstituted arylthio group, a substituted orunsubstituted alkylsulfoxy group, a substituted or unsubstitutedarylsulfoxy group, a substituted or unsubstituted alkenyl group, asubstituted or unsubstituted amine group, a substituted or unsubstitutedaryl group, or a substituted or unsubstituted heterocyclic group; l is amole fraction and is a real number of 0<l<1; m is a mole fraction and isa real number of 0<m<1; l+m=1; and n is a repetition number of the unitand is an integer of 1 to 10,000.
 9. The composition for an organicmaterial layer of an organic solar cell of claim 1, wherein the polymerincludes a unit of any one of Chemical Formulae 5-3-1 to 5-3-3:

wherein: A1 to A4 are the same as or different from each other, and areeach independently a halogen group; R107, R108, R207 and R208 are thesame as or different from each other, and are each independently asubstituted or unsubstituted alkoxy group; R111, R112, R211 and R212 arethe same as or different from each other, and are each independently asubstituted or unsubstituted alkyl group, a substituted or unsubstitutedsilyl group, or a substituted orunsubstituted alkylthio group; R411 andR412 are the same as or different from each other, and are eachindependently a substituted or unsubstituted alkyl group or asubstituted or unsubstituted alkoxy group; l is a mole fraction and is areal number of 0<l<1; m is a mole fraction and is a real number of0<m<1; l+m=1; and n is a repetition number of the unit and is an integerof 1 to 10,000.
 10. The composition for an organic material layer of anorganic solar cell of claim 1, wherein the polymer includes a unit ofany one of Chemical Formulae 5-4 to 5-60:

wherein: l is a mole fraction and is a real number of 0<l<1; m is a molefraction and is a real number of 0<m<1; l+m=1; and n is a repetitionnumber of the unit and is an integer of 1 to 10,000.
 11. An organicsolar cell comprising: a first electrode; a second electrode on thefirst electrode; and one or more organic material layers between thefirst electrode and the second electrode, the one or more organicmaterial layers including a photoactive layer, wherein the one or moreorganic material layers include the composition of claim
 1. 12. Theorganic solar cell of claim 11, wherein the electron donor and theelectron acceptor form a bulk heterojunction (BHJ).
 13. The compositionfor an organic material layer of an organic solar cell of claim 1,wherein the second unit is a unit of Chemical Formula 2-2:


14. The composition for an organic material layer of an organic solarcell of claim 1, wherein the third unit is a unit of Chemical Formula3-5:

wherein: R7 and R8 have the same definitions as in Chemical Formula 3;and R19 is hydrogen, a substituted or unsubstituted alkyl group, asubstituted or unsubstituted alkoxy group, a substituted orunsubstituted aryloxy group, a substituted or unsubstituted alkylthiogroup, a substituted or unsubstituted arylthio group, a substituted orunsubstituted aryl group, or a substituted or unsubstituted heterocyclicgroup.